Adhesion molecule expression on eosinophils in idiopathic eosinophilic pneumonia

被引:13
作者
Azuma, M [1 ]
Nakamura, Y [1 ]
Sano, T [1 ]
Okano, Y [1 ]
Sone, S [1 ]
机构
[1] UNIV TOKUSHIMA,SCH MED,DEPT INTERNAL MED 3,TOKUSHIMA 770,JAPAN
关键词
adhesion molecules; bronchoalveolar lavage fluid; eosinophils; idiopathic eosinophilic pneumonia; intercellular adhesion molecule-1;
D O I
10.1183/09031936.96.09122494
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Idiopathic eosinophilic pneumonia (IEP) is characterized by the accumulation of eosinophils in the alveolar spaces and the interstitium of the lung, frequently accompanied by peripheral eosinophilia. To clarify the roles of adhesion molecules of eosinophils in the pathogenesis of eosinophilic pneumonia, we analysed their expression by eosinophil and T-lymphocyte populations in peripheral blood and bronchoalveolar lavage fluid (BALF) obtained from 11 patients with eosinophilic pneumonia, using flow cytometric methods. Cell differentials in BALF showed increased numbers of eosinophils, the increase correlating with the number of activated T-lymphocytes in BALF. The expressions of CD11a (lymphocyte function-associated antigen-1 (LFA-1)), CD11b (Mac-1), CD18, CD49d (very late activation antigen-4 (VLA-4)), and CD62L (L-selectin) by eosinophils in BALF were all. lower than those of eosinophils in peripheral blood. In contrast, CD54 (intercellular adhesion molecule-1 (ICAM-1)) was expressed by eosinophils in BALF, but not by those in peripheral blood. These results indicate that intercellular adhesion molecule-1 expression by eosinophils in bronchoalveolar lavage fluid but not in peripheral blood may be induced by locally activated T-celIs or macrophages and may be important in the pathogenesis of idiopathic eosinophilic pneumonia.
引用
收藏
页码:2494 / 2500
页数:7
相关论文
共 37 条
[1]   ACTIVATED AND MEMORY ALVEOLAR T-LYMPHOCYTES IN IDIOPATHIC EOSINOPHILIC PNEUMONIA [J].
ALBERA, C ;
GHIO, P ;
SOLIDORO, P ;
MABRITTO, I ;
MARCHETTI, L ;
POZZI, E .
EUROPEAN RESPIRATORY JOURNAL, 1995, 8 (08) :1281-1285
[2]   PULMONARY EOSINOPHILS EXPRESS HLA-DR IN CHRONIC EOSINOPHILIC PNEUMONIA [J].
BENINATI, W ;
DERDAK, S ;
DIXON, PF ;
GRIDER, DJ ;
STROLLO, DC ;
HENSLEY, RE ;
LUCEY, DR .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1993, 92 (03) :442-449
[3]   EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039
[4]   CYTOKINES IN SYMPTOMATIC ASTHMA AIRWAYS [J].
BROIDE, DH ;
LOTZ, M ;
CUOMO, AJ ;
COBURN, DA ;
FEDERMAN, EC ;
WASSERMAN, SI .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :958-967
[5]  
CLUTTERBUCK EJ, 1989, BLOOD, V73, P1504
[6]   INDUCTION OF INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) EXPRESSION IN NORMAL HUMAN EOSINOPHILS BY INFLAMMATORY CYTOKINES [J].
CZECH, W ;
KRUTMANN, J ;
BUDNIK, A ;
SCHOPF, E ;
KAPP, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 100 (04) :417-423
[7]   EOSINOPHILIC PNEUMONIA WITHOUT RADIOGRAPHIC PULMONARY-INFILTRATES [J].
DEJAEGHER, P ;
DERVEAUX, L ;
DUBOIS, P ;
DEMEDTS, M .
CHEST, 1983, 84 (05) :637-638
[8]  
EBISAWA M, 1992, J IMMUNOL, V149, P4021
[9]  
ELIAS JA, 1985, J IMMUNOL, V135, P3198
[10]  
FUKUDA T, 1994, J ALLERGY CLIN IMMUN, V93, P269